Ethyl Acetate → HCID 19848771, compound

HRID 1607453Notes

Reaction equation

HRID 1607453 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C[O:8]C1C=C(CNCCCNCCCCNCCCN)C=CC=1O.O[C:32]1([CH3:58])[CH2:37][CH:36]([CH:38]([CH3:42])[CH2:39][C:40]#[N:41])[C:35]2[CH:43]=[CH:44][C:45]([CH:47]([CH2:49][CH2:50][CH2:51][C:52]3[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=3)[CH3:48])=[CH:46][C:34]=2[O:33]1.C(OCC)(=O)C>O1CCCC1>[NH2:41][CH2:40][CH2:39][CH:38]([CH:36]1[C:35]2[C:43]([OH:8])=[CH:44][C:45]([CH:47]([CH2:49][CH2:50][CH2:51][C:52]3[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=3)[CH3:48])=[CH:46][C:34]=2[O:33][CH:32]([CH3:58])[CH2:37]1)[CH3:42]

Participants

5

Procedure

Under anhydrous conditions and a nitrogen atmosphere, to a solution of 190 mg (5 mmole) lithium aluminum hydride in 50 ml tetrahydrofuran at 10° C. is added dropwise a solution of 1.885 g (5 mmole) dl-5-hydroxy-4-(1-methyl-2-cyanoethyl)-2-methyl-7-(5-phenyl-2-pentyl)-3,4-dihydro-2H-benzopyran in 25 ml of tetrahydrofuran. After the addition is complete, the mixture is stirred at room temperature for 6 hours. Ethyl acetate is added to consume the unreacted hydride. The reaction mixture is evaporated to dryness, the residue partitioned between water and methylene chloride and the organic layer dried over anhydrous magnesium sulfate. The solvent is evaporated to provide the title compound as the free base.

Workup

  1. additionAfter the addition
  2. customto consume the unreacted hydride
  3. customThe reaction mixture is evaporated to dryness
  4. customthe residue partitioned between water and methylene chloride
  5. dry with materialthe organic layer dried over anhydrous magnesium sulfate
  6. customThe solvent is evaporated

Sources & evidence

ORD record
ord-a81d11210d3e47559d4bcce0ca87e353
Source dataset
uspto-grants-1989_09
Patent number
US04863934

Reaction notes

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